| Literature DB >> 33061316 |
Rob A B Oostendorp1,2,3,4, J W Hans Elvers5,6, Emiel van Trijffel7,8, Geert M Rutten9,10, Gwendolyne G M Scholten-Peeters11, Marcel Heijmans4, Erik Hendriks12,13, Emilia Mikolajewska14,15, Margot De Kooning3,16, Marjan Laekeman17,18, Jo Nijs3,16,19, Nathalie Roussel20, Han Samwel21.
Abstract
BACKGROUND: Whiplash-associated disorders (WADs) constitute a state of health characterized by a wide diversity of symptoms as a result of impairments of functions, activity limitations, and participation restrictions. Patient-reported outcome measurements (PROMs) and patient-reported outcomes (PROs) seem appropriate when describing and evaluating the health status of patients with WAD. AIM: To measure the use of PROMs and PROs as quality indicators in clinical reasoning, and to analyze and evaluate pre- and post-treatment 'pain intensity' and 'functioning', and for 'perceived improvement' in patients with WAD in primary care physiotherapy practice by year of referral, with the phase after accident and prognostic health profile embedded in the clinical reasoning process.Entities:
Keywords: neck pain; patient-reported outcomes measures; physiotherapy; routinely collected data; whiplash-Associated Disorders
Year: 2020 PMID: 33061316 PMCID: PMC7532902 DOI: 10.2147/PPA.S262578
Source DB: PubMed Journal: Patient Prefer Adherence ISSN: 1177-889X Impact factor: 2.711
Phase- and Profile-Based Treatment Goals and Physiotherapy Treatment Modalities, Together with Outcomes for Management in Patients with Whiplash-Associated Disorders (WAD)
| Phase After Whiplash-Related Injurya, Combined with Prognostic Health Profileb | Treatment Goals | Interventionsc | Outcomes |
|---|---|---|---|
| Phase 1 (<7 days) | Reducing pain | Education | Patient-reported outcomes. Pain intensity. Functioning/Activity limitations. Perceived recovery. Return to work participation |
| Phase 2 (1–3 weeks) | See Phase 1 + improving musculoskeletal function | See Phase 1 | |
| Phase 3 (4–6 weeks) | See Phase 2 + increasing activities and participation | See Phase 1 | |
| Phase 3 (4–6 weeks) | Explaining underlying pain mechanisms | Pain education | |
| Phase 4 (7–12 weeks) | See Phase 3a + minimizing delay in work participation | See Phase 3a | |
| Phase 4 (7 −12 weeks) | See Phase 3b | See Phase 3b | |
| Phase 5 (3–6 months) | See Phase 3b | See Phase 4 | |
| Phase 6 (>6 months) | See Phase 3b | See Phase 5 |
Notes: aPhases after whiplash-related injury: Phase 1: <7 days; acute; normal recovery: Phase 2: 1–3 weeks; acute; normal recovery: Phase 3a: 4–6 weeks; sub-acute; inconclusive recovery: Phase 3b: 4–6 weeks; sub-chronic; delayed recovery: Phase 4a: 7–12 weeks; sub-acute; inconclusive recovery: Phase 4b: 7–12 weeks; sub-chronic; delayed recovery: Phase 5: 3–6 months; chronic; no recovery: Phase 6: >6 months; chronic; no recovery: bPrognostic health profile: Profile A: normal recovery, low intensity of pain, decreasing pain, increasing activities, active coping, no fear avoidance: Profile B: inconclusive recovery, middle intensity of pain, persistent pain, persistent activity limitations, inconclusive coping, inconclusive fear avoidance: Profile C: delayed recovery, high intensity of pain, increasing pain, decreasing activities, passive coping, fear avoidance: cClassification Allied Health Care, version Physiotherapy: 1. History Taking; 2. Inspection and observation; 3. Palpation; 4. Active exercise therapy; 5. Passive exercise therapy (manual therapy); 6. Massage therapy; 7. Modalities of physical therapy (ie, low- and high-frequency electrotherapy); 8. Coaching; 9. Education.
Baseline Characteristics in Physiotherapy Management in Patients with Whiplash-Associated Disorders
| Total n=523: n (%) Unless Otherwise Stated | |
|---|---|
| Sociodemographic characteristics | |
| Age (year) (mean; SD)
Female Male | |
| Gender (female) | 396 (75.7) |
| Educational level
Lower (primary school) Intermediate (secondary school) Higher (post-secondary school) | |
| Employment status
Unemployed/job seeking In work Retired | |
| Accident-related characteristics | |
| Direction of impact (back) | 356 (68.2) |
| Anticipated collision (no) | 414 (79.2) |
| Type of trauma
Neck Neck and head Other type | |
| Classification WADa WAD-1 WAD-2 WAD-3 WAD-4 | |
| Period since accident
<7 days 1–3 weeks 4–6 weeks 7–12 weeks 3–6 months >6 months | |
| Onset of symptoms
Immediately ≤2 days 3–7 days >1 week | |
| Pre-existing health status | |
| Functioning problems
Activity limitation (yes) Participation problems (yes) Job-related problems (yes) | |
| Relevant medication use (yes) | 74 (14.1) |
| Previous whiplash injury (yes) | 55 (10.5) |
| Previous neck pain and stiffness (yes) | 96 (18.4) |
| Pain elsewhere (yes) | 115 (22.0) |
| Previous diagnostics and treatment | |
| Medical imaging diagnostics (yes) | 90 (17.2) |
| Cervical soft collar (yes)
Weeks (mean; SD) | 295 (56.4) |
| Pain medication (yes) | 221 (42.3) |
| (Manual) physiotherapy (yes; n=234)
Active exercise therapy Manual therapy Active exercise therapy + manual therapy Massage therapy Combined therapy | |
| Recovery after treatment
Fully Partially Stabilization Deterioration Inconclusive | |
| Current health status and recovery rate | |
| Recovery since accident
Normal Inconclusive Deterioration | |
| Functioning problems
Impairments in musculoskeletal neck functions (yes) Activity limitation (yes) Participation problems (yes) Job-related problems (yes) | |
| Pain medication (yes) | 131 (25.0) |
| Type and number of symptoms
≤3: neck pain, stiffness, decreased ROMb 4–6: + dizziness, headache and tinnitus 7–9: + cognitive impairments >9: + rest | |
| Pain intensity (VAS-P ≥55 mm; 0–100 mm)c | 330 (63.1) |
| Functioning (NDI >29%; 0–50 points)d | 514 (98.3) |
| Current pain behavior and fear avoidance | |
| Observation pain behavior (yes) | 510 (97.5) |
| Modified Waddell’s non-organic physical signse ≤3 >3 | |
| Pain Coping Inventorye PCI-Active (score: 12–48) (mean; SD) Active coping (score ≥24) PCI-Passive (score 21–84) (mean; SD) Passive coping (score ≥42) | |
| Fear Avoidance Beliefs Questionnairef FABQ-Activities (score: 0–24) (mean; SD) Risk for pain avoiding behavior (score >15) FABQ-Work (score: 0–42) (n=354) (mean; SD) Risk for no return to work (score >34) | |
Notes: aClassification WAD: Whiplash-Associated Disorders: WAD 0: no neck symptoms, no physical sign(s); WAD 1: neck pain, stiffness or tenderness only, no physical sign(s); WAD 2: neck symptoms and musculoskeletal sign(s); WAD 3: neck symptoms and neurological sign(s); WAD 4: neck symptoms and fracture or dislocation bROM: Range of Motion. cVAS-P: Visual Analogue Scale for Pain: horizontal line of 100 mm scored from 0 (no pain) to 100 (worst imaginable pain). dNDI: Neck Disability Index: 10 items scored from 0 (no activity limitation) to 5 (major activity limitation); total score 0–50. eModified Waddell’s non-organic physical signs: superficial tenderness, non-anatomical tenderness, pain simulation test, cervical ROM, regional disturbance, overreactionePain Coping Inventory (PCI): 33-item questionnaire measuring active coping (PCI-Active: 12 items [12–48]; ≥24 active coping) and passive coping (PCI-P: 21 items [21–84]; ≥42 passive coping). Items are scored on a 4-point Likert scale ranging from 1 (hardly ever) to 4 (very often). fFear Avoidance Beliefs Questionnaire (FABQ): 16-item questionnaire measuring fear avoidance beliefs related to physical activities (FABQ-Activities: 4 items [0–24]; >15 at risk for pain avoiding behavior), and work-related activities (FABQ-Work: 7 items [0–42]; >34 at risk for no return to work). Items are scored on a 7-point Likert scale ranging from 0 (completely disagree) to 6 (completely agree)
10 Year Related Outcomes for Physiotherapy Management in Patients with Whiplash-Associated Disorders (WAD) (n=523)
| Year of Referrala | Pain Intensityb | Functioning | Perceived Improvementd | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| n (%) | Pre-treatment score | Post-treatment score | Effect size# | Difference | MCID | Pre-treatment score | Post-treatment score | Effect size# | Difference | MCID | Improved | No change | Worse |
| 1 (n=66) | 56.1 (17.6) | 27.7 (17.6) | 1.61 | 28.4* | 54 | 27.9 | 13.1 | 1.64 | 14.8* | 49 | 31 | 24 | 11 |
| 2 (n=57) | 59.6 (14.8) | 29.2 (14.5) | 2.07 | 30.4* | 51 | 29.5 | 16.4 | 1.70 | 13.1* | 37 | 29 | 22 | 6 |
| 3 (n=48) | 57.5 (13.5) | 30.8 (11.6) | 2.12 | 26.7* | 35 | 27.5 | 14.3 | 2.01 | 13.2* | 34 | 21 | 16 | 11 |
| 4 (n=50) | 59.1 (14.7) | 28.9 (10.3) | 2.38 | 30.3* | 40 | 29.7 (6.9) | 16.6 (7.0) | 1.88 | 12.8* | 32 | 22 | 21 | 7 |
| 5 (n=30) | 58.5 (11.2) | 33.2 (13.7) | 2.02 | 25.2* | 25 | 27.8 (5.7) | 17.0 (9.0) | 1.43 | 10.8* | 16 | 9 | 18 | 3 |
| 6 (n=43) | 56.1 (12.8) | 30.7 (14.4) | 1.86 | 25.4* | 35 | 27.4 (5.9) | 17.1 (9.0) | 1.35 | 10.3* | 21 | 18 | 17 | 8 |
| 7 (n=44) | 59.6 (16.0) | 32.9 (13.8) | 1.79 | 26.8* | 34 | 29.4 (8.9) | 18.3 (9.5) | 1.21 | 11.1* | 24 | 14 | 18 | 12 |
| 8 (n=60) | 53.4 (11.7) | 27.4 (11.8) | 2.21 | 25.9* | 50 | 25.4 (6.6) | 14.1 (7.3) | 1.61 | 11.3* | 33 | 29 | 19 | 12 |
| 9 (n=58) | 58.4 (14.4) | 29.5 (13.8) | 2.05 | 29.0* | 51 | 28.6 (7.9) | 16.5 (9.8) | 1.36 | 12.1* | 31 | 31 | 20 | 7 |
| 10 (n=67) | 59.9 (15.0) | 28.9 (11.1) | 2.07 | 31.1* | 63 | 29.1 (7.9) | 17.0 (8.8) | 1.45 | 12.2* | 35 | 37 | 24 | 6 |
| Total (n=523) | 57.8 (14.5) | 29.6 (13.5) | 2.01 | 28.2* | 443 | 28.2 (7.5) | 15.9 (8.6) | 1.52 | 12.3* | 312 | 241 | 199 (38.0) | 83 |
Notes: aYear of referral: 2002–2011 (1-10). bPain intensity: Visual Analogue Scale for Pain (VAS-P): horizontal line of 100 mm scored from 0 (no pain) to 100 (worst imaginable pain). #Effect size: Cohen’s d 0.21–0.50 small; 0.51–0.80 medium; >0.81 large. *Statistical significance P< 0.001 (paired sample t-test; individual delta pre-post) MCID: Minimal Clinically Important Difference: VAS-P ≥30% of pretreatment score (mm). cFunctioning/Activity limitation: Neck Disability Index (NDI): 10 items scored from 0 (no activity limitation) to 5 (major activity limitation); total score 0–50 points. # Effect size: see Pain Intensity. *Statistical significance: see Pain Intensity MCID: Minimal Clinically Important Difference: NDI ≥11 points dGlobal Perceived Effect: “improved” (’complete improved’; “much improved”; “slightly improved”); “no change”; “worse” (slightly worse’; “much worse”).
Phase-Related Outcomes for Physiotherapy Management in Patients with Whiplash-Associated Disorders (WAD) (N=523)
| Phases After Whiplash-Related Injurya | Pain Intensityb | Functioning | Perceived Improvementd | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| n (%) | Pre- treatment | Post-treatment | Effect size# | Difference | MCID | Pre-treatment score | Post-treatment score | Effect size# | Difference | MCID | Improved | No change | Worse |
| Phase 1 | 47.5 | 21.2 | 1.54 | 26.3* | 12 | 22.4 | 10.6 | 1.28 | 12.1* | 8 | 9 | 4 | 1 |
| Phase 2 | 57.5 | 30.0 | 1.99 | 27.6* | 78 | 28.4 | 15.0 | 1.73 | 13.4* | 67 | 39 | 43 | 16 |
| Phase 3 | 56.7 | 28.7 | 1.74 | 28.2* | 102 | 27.6 | 15.7 | 1.29 | 12.2* | 73 | 54 | 43 | 21 |
| Phase 4 | 57.9 | 29.1 | 2.20 | 28.8* | 98 | 28.4 | 16.1 | 1.56 | 12.3* | 66 | 60 | 39 | 15 |
| Phase 5 | 57.8 | 30.0 | 2.18 | 27.7* | 105 | 28.3 | 16.0 | 1.69 | 12.2* | 68 | 54 | 50 | 19 |
| Phase 6 | 63.0 | 33.2 ( | 2.41 | 29.7* | 46 | 30.3 | 18.9 | 1.42 | 11.3* | 30 | 25 | 20 | 11 |
| Total | 57.8 | 29.6 | 2.01 | 28.2* | 443 | 28.2 | 15.9 | 1.52 | 12.3 | 312 | 241 | 199 | 83 |
Notes: aPhase after whiplash-related injury: Phase 1: <7 days; acute; normal recovery Phase 2: 1–3 weeks; acute; normal recovery Phase 3a: 4–6 weeks; sub-acute; inconclusive recovery Phase 3b: 4–6 weeks; sub-chronic; delayed recovery Phase 4a: 7–12 weeks; sub-acute; inconclusive recovery Phase 4b: 7–12 weeks; sub-chronic; delayed recovery Phase 5: 3–6 months; chronic; no recovery Phase 6: > 6 months; chronic; no recovery. bPain intensity: Visual Analogue Scale for Pain (VAS-P): horizontal line of 100 mm scored from 0 (no pain) to 100 (worst imaginable pain) # Effect size: Cohen’s d 0.21–0.50 small; 0.51–0.80 medium; >0.81 large *Statistical significance P< 0.001 (paired sample t-test; individual delta pre-post) -MCID: Minimal Clinically Important Difference: VAS-P ≥30% of pretreatment score (mm). cFunctioning/Activity limitation: Neck Disability Index (NDI): 10 items scored from 0 (no activity limitation) to 5 (major activity limitation); total score 0–50 points -#Effect size: see Pain Intensity* Statistical significance: P< 0.001 (paired sample t-test; individual delta pre-post) MCID: Minimal Clinically Important Difference: NDI ≥11 points. dGlobal Perceived Effect: perceived improvement -“improved” (’complete improved’; “much improved”; “slightly improved”); “no change”; “worse” (slightly worse’; “much worse”).
Health Profile-Related Outcomes for Physiotherapy Management in Patients with Whiplash-Associated Disorders (WAD) (n=523)
| Health Profilea | Pain Intensityb | Functioning | Perceived improvementd | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| n (%) | Pre-treatment score | Post-treatment score | Effect size# | Difference | MCID | Pre-treatment score | Post-treatment score | Effect size# | Difference | MCID | Improved | No change | Worse |
| Profile A | 40.8 | 13.9 | 1.89 | 26.9* | 37 | 20.6 | 7.4 | 1.60 | 13.2* | 27 | 34 | 4 | 2 |
| Profile B | 55.6 | 29.4 | 2.23 | 26.2* | 277 | 27.2 | 15.4 | 1.66 | 11.8* | 194 | 150 (44.2) | 135 | 54 |
| Profile C | 67.5 | 34.4 | 2.40 | 33.3* | 125 | 32.7 | 19.3 | 1.65 | 13.4* | 91 | 57 | 68 | 27 |
| Total (n=523) | 57.8 | 29.6 | 2.01 | 28.2* | 443 | 28.2 | 15.9 | 1.52 | 12.3* | 312 | 241 (46.1) | 199 | 83 |
Notes: aPrognostic health profile: Profile: normal recovery, low intensity of pain, decreasing pain, increasing activities, active coping, no fear avoidance Profile B: inconclusive recovery, middle intensity of pain, persistent pain, persistent activity limitations, inconclusive coping, inconclusive fear avoidance -Profile C: delayed recovery, high intensity of pain, increasing pain, decreasing activities, passive coping, fear avoidance. bPain intensity: Visual Analogue Scale for Pain (VAS-P): horizontal line of 100 mm scored from 0 (no pain) to 100 (worst imaginable pain) -#Effect size: Cohen’s d 0.21–0.50 small; 0.51–0.80 medium; >0.81 large *Statistical significance P< 0.001 (paired sample t-test; individual delta pre-post) MCID: Minimal Clinically Important Difference: VAS-P ≥30% of pretreatment score (mm). cFunctioning/Activity limitation: Neck Disability Index (NDI): 10 items scored from 0 (no activity limitation) to 5 (major activity limitation); total score 0–50 points #Effect size: see Pain Intensity*Statistical significance: P< 0.001 (paired sample t-test; individual delta pre-post) MCID: Minimal Clinically Important Difference: NDI ≥11 points. dGlobal Perceived Effect: perceived improvement “improved” (’complete improved’; “much improved”; “slightly improved”); “no change”; “worse” (slightly worse’; “much worse”).